#Apartments for the whole family in Metairie LA

[indianroseeee-blog]

I could still feel the tears falling down my face as my rhuematologist told me that i have been diagnosed with Lupus. I blamed everyone. When I found out it can also be genetic. I dropped because my mother is also dealing with the same condition i had. I sometimes chose not to talk and hold so much anger inside when i was mostly needed to relax and not stressed. I felt that my life would be over with. I graduated in 2013 from L W Higgins High School and moved in my apartment the following year. 

Around this time i was also in school and working two jobs. My husband had a job also. Then one day i was working at Walmart as a cashier. I was scanning someones order and almost passed out. She asked me was i ok and i told her no i really didn't feel good. So i went home and laid in my bed feeling like i just ran 5 miles. Around this time my bipolar tendencies started to kick in because i was scared and paranoid. Every time i get sick i always go to talk like i am about to die. I realize there is much more i wanna live for. 

One day in the middle of the night, i woke my husband up from his sleep. i had so much excruciating pain that i could not hold myself up. He thought i was being over dramatic but i was being very honest. But , he still ended up bringing me to the hospital. There we set and waited for a hour in the waiting room at Oschner ER in Kenner,LA. The kept saying it was a urinary tract infection. so they prescribed me antibiotics that had sulfate in it. I took the pill and went to bed. I woke up again and begged my husband to bring me back to the ER because i was suffocating. I caught an allergic reaction and my glands and airway swelled. They gave me medicine and told me tried to get rid of it the natural way. I went to another emergency hospital called East Jefferson Hospital in Metairie, LA.. They were saying the same thing. That night i went home and begin to eat and it would run straight through me. Like literally sometimes i couldn't even make it to the bathroom. Or sometimes when i feel the urge to pee, my body starts to make me pee. I had no control over my body what so ever. 

I was taking a bath in all hot water and it wasn't burning me, but it was hurting my husband to help bathe me. For the next few days i would sleep all day. I couldnt eat because i couldn't hold anything down. i would have really bad sweat episodes to where my body sweat imprint would be soaked within  the bed. Then i couldn't breathe laying down, so i sat up to go to sleep. Around 12:30 at night i squealed my husbands name and he didn't here me and i said it one more time and woke up. I told him that i couldn't breathe and he carried me from our upstairs apartment to the car. He was so worried he kept telling me to respond to him. I began to go in and out of consciousness. By this time, My whole face swelled to where i couldn't see anything. By the now the nurses know me by heart.

i was rushed to the back. My BP (blood pressure) was 98/52. which is not good. The ER doctor called the admitting doctor because he told me he didn't know what was going on and i have been coming back and forth here between the last two weeks. They admitted me and it took them almost two months of me being in the hospital, that it was my kidneys. My kidneys were failing. So at first they had me on 60 MG Prednisone & Imuran & plaquinil. Then they switched me to cellcept. My body started to regulate again. By this time i lost everyone because of me not being able to work because of how sick i was.I couldn't even finish school semester all because i was in the hospital. I felt like there was nothing left. I felt as if now i became a burden on others and i never wanted someone to feel like they were obligated to take care of me. 

When my husband watch the lady trying to put and IV in my vein, he broke down. The nurse told me that she was gonna stick me and i didn't move or respond. She ask me did i feel anything and i said no. My body was not respond to pain or touch. 

i ended up in that hospital unable to move. 

Then came my second kidney failure which was completely different from the first one. In feb of 2016 i was in an accident where the lady hit me head on.I was vomiting up blood, blood clots eroded from my skin, alopecia, Skin rash over entire body, Peeling like a new born baby. My skin would heal, peel, bleed, infect, heal, and repeat again. This took about a year. Around this time i had gained 60 pounds i would say or more in retention fluid.i would have the worse muscle spasms. When i went to the ER i kept getting pumped with narcotics until they figured out the problem.  

Sometimes it would be so bad that it started to affect my work, i would always be late to class because the fluid was taking over my body.it was painful to walk, because the fluid is applying pressure. i would vomit blood. i was going to the ER every two days. It was horrible. i retained so much fluid that it affected my sex life and brought my body through changes. My vagina had completely swelled and it burned to pee a little, i didn't know what to do. My skin cam completely sunburned on my vagina it looked like. It was swollen so bad that my husband could not have sex with me cause i was so swollen. He did and he takes great care of me. When my vagina swelled it got worser. I started to feel like i had a booty in the front and back.When i slept i had to lay a towel down because the fluid started seeping through my skin. My mother would just sit that and run her fingers through my hair and cried. It was my kidneys again. i started a chemo infusion called Rutuxinmab. Dr. Stephen Morse (Nephrologist) of LSU family practice & Louis Espinoza (Rhuematologist) of LSU family practice saved my life.

my skin would dry out even with lotioning my body. i would have to lotion my body two times to three times a day. Then it had to be non scented lotion. Like Cetaphil. i bath in every that didn't have a fragrance and  will post more blogs about that to come. I would only take lukewarm bathes and i would wash myself twice. When having a open sore , always keep it wrapped. Around this time i had to quit working and i could not even go to school. Each time they made me payback to school. I would bring medical records and all of what happened. I even provided pictures. It was weird cause they granted a refund to her when her grandmother passed. I felt sad because what was happening was something i couldn't control. Then i moved to Dallas,TX and I was in the hospital at first for two weeks cause i had a flare up and i told them i had lupus but thats all they know. They really didn't take the trusting their patients seriously. They asked me what was my old hospital information and i told them but the hospital i was at did not but only mailed. So i waited about two weeks but in the meantime i told them to do a kidney biopsy. This would have been my second one. 

Ladies and gentlemen , this procedure can be done while woke. But after the procedure you can not leave the bed for 6 hours, so i slept. They told me to take it easy and i didn't understand really because my first kidney biopsy i was up and about right after i left. But this one was different my back was in so much pain i was knocking myself out. A Few weeks later they got my info. They wanted to contact me but when they found me in the ER they were ready to talk to me. They told be it was Stage 5, but it was only 20% damaged and 80% percent good. We think we can make this go into remission. They also asked me why am i vomiting blood and i told him i didn't know it must have been my gastritis. so they did ANOTHER endoscopy . Its when they inserted a tube down your through to your abdomen to see if they say abnormalities. This procedure ofcourse you was kicked out. But this was worst. When i woke up i my lip was in so much pain. Y'all i bit my lip. I mean it look like someone knocked my ass out. I was like what happened? and they told me that  happened sometimes during the procedure and i said oh never with the first one i didn't though. Then y'all guess what, i said why am i so wet? They told me sometimes the patients pee a little during the procedure. 

Well guess what it wasnt not piss , it was shit , LMAO!! yo , i told the lady , “ y'all know y'all offed up, y'all could at least told me i shitted on myself, can i get stuff to wash my shitty ass ,LMAO i was so embarrassed. I was like why lord. But overall i haven't been in the hospital but I'm not into full remission yet. and my doctors know what i want my future plan to be and I'm fine with that. So now we are currently working on getting me off these meds. :) 

[latitudeapartments]

Luxury Apartments at Latitude | Rent Apartments New Orleans

Welcome to Latitude

Latitude is an upcoming residential tower designed to deliver an aspiring lifestyle to the urban nomad. This 196-unit complex, being built in Metairie, Louisiana, is conveniently located on Lake Pontchartrain's south shore near New Orleans. Often touted to be one of the best places to live in Louisiana, Metairie's spirit of a mixed urban-suburban feel is captured beautifully in Latitude's architectural design.

The city exudes a unique cross-cultural charm making it a favorite tourist spot and a proud home to many enjoying its arts, unique entertainment profile, and French-accented Southern grace. Surrounded by water—the lake to the north and the Mississippi River to the south—and papered with parks, entertainment venues, and historic businesses and eateries. There are a lot of bars, restaurants, and coffee shops frequented by locals and tourists alike.

Latitude is located at 3100 Lake Villa Drive at the intersection of Rye Street and is easily accessible by Interstate-10. And is minutes away from many major employers as well as shopping, dining, and entertainment.

Visit Us: 3100 Lake Villa Dr, Metairie, Louisiana. Call: +1 985 618 1600 Email: contact@latitude.apartments

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